Long-read Sequencing Uppsala (LRUA) 2022
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In recent years, long-read DNA sequencing technologies have replaced short-read sequencing as the gold standard solution for a wide range of genomics applications. In addition to producing high quality de novo genome assemblies, long-read technologies can be used to study complex structural variation, full-length RNA isoforms, detection of epigenetic signals, and much more. The adaptation of long-read sequencing is sweeping through several areas of the life sciences including agricultural, environmental, and medical research.
Join us in Uppsala to catch up with the latest developments in long-read sequencing technologies and their applications, get inspired by peers presenting their research, and enjoy discussions with leading experts and company representatives.
You can hear from Oxford Nanopore Technologies at the following times.
10:50 - 11:15, Monday 31st October - Tonya McSherry 'One platform for multinomics - where will nanopore sequencing take you?'
09:00 - 10:00, Wednesday 2nd November - Oxford Nanopore Technologies Workshop 'Experience real-time nanopore sequencing and analysis live'
This is an in person conference, registration is required.
